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NCT06940687Completed

Neurophysiological Benefits of Live Music for Early Alzheimer's Patients and Their Caregivers

Source: ClinicalTrials.gov · Last updated 19 Oct 2026

Brief summary (registry, in English)

This study aims to investigate the neurophysiological effects of live music on individuals with early Alzheimer's Disease (AD), dementia, and/or mild cognitive impairment (MCI) and their caregivers. Heart rate (HR), heart rate variability (HRV), and brain activity will be measured as participant-caregiver dyads listen to preferred and improvised music performed by professional musicians. Investigators will leverage various measurement techniques including, but not limited to, electroencephalography (EEG), behavioral, surveys, and physiological monitoring to study the impact of live music on anxiety in AD and inter-dyad synchrony.

Status (registry)
Completed
Study type
Interventional
Enrollment
10 (actual)
First submitted
19 Feb 2025
Start date
28 Jan 2025
Primary completion date
27 Aug 2026
Lead sponsor
Yale University
NCT number
NCT06940687

What you commit to

  • Study type: Interventional
  • Participants enrolled: 10
  • From 28 Jan 2025 to the primary completion date, 27 Aug 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Starting a new prescription medication in the last 6 months

Other illness

  • Clinical Dementia Rating \<0.5 or \> 2
  • Participating in another clinical trial studying AD and/or Dementia

Other

  • Unable to provide informed consent
  • Endorsing suicidal ideation (SI), self-injurious behavior, or homicidal ideation (HI) above the threshold defined in the "Risk Reduction and Safety Plan"
  • Prescribed Benzodiazepines on an as needed basis

Who the study is looking for

  • Clinical Dementia Rating 0.5 - 2
  • Be a person with or caregiver to a person with a diagnosis of early Alzheimer's Disease, mild dementia, and/or mild cognitive impairment (MCI)
  • Able to provide informed consent
  • Willing to wear an EEG headset and heart rate monitoring devices
  • Willing to possibly have small patches of body / facial hair shaved to accommodate administration of heart rate monitoring devices
  • Willing to answer survey questions about topics related to the study
  • Willing to be audio / video recorded

Age in the registry: 50 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Firehouse 12 Studios
Coordinator of this site? Confirm its status
New HavenUnited StatesUnknown status
Musical Intervention Studios
Coordinator of this site? Confirm its status
New HavenUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.